Craig J. Morton

The paper identifies potent reaction hijacking inhibitors targeting Plasmodium falciparum asparagine tRNA synthetase, showing high selectivity and resistance refractoriness.

The paper presents a cryo-EM structure of the PorKN rings and shows their interaction with PorG and Attachment Complexes, proposing a mechanism for protein secretion in the Type IX Secretion System.

This study identifies Plasmodium aspartyl-tRNA synthetase as an antimalarial target by showing how natural products inhibit protein translation through reaction hijacking.

This study identifies distinct roles of PGRL1 paralogs in photoprotection within C4 photosynthesis, showing PGRL1{beta} enables rapid photoprotection while PGRL1 maintains oxidation under steady-state high light.